A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18056433



Internal ID20623474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19599367..19601845hg38UCSC Ensembl
chr1:19925861..19928339hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg382479
hg192479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316568
Supporting Variants
Samples
Known GenesMINOS1, MINOS1-NBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18056433
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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